Effectiveness of fosfomycin tromethamine prophylaxis in preventing infection following transrectal ultrasound-guided prostate needle biopsy: Results from a large Canadian cohort.


Journal

Journal of global antimicrobial resistance
ISSN: 2213-7173
Titre abrégé: J Glob Antimicrob Resist
Pays: Netherlands
ID NLM: 101622459

Informations de publication

Date de publication:
06 2019
Historique:
received: 24 10 2018
revised: 21 11 2018
accepted: 27 11 2018
pubmed: 16 12 2018
medline: 19 6 2020
entrez: 16 12 2018
Statut: ppublish

Résumé

Rates of infection following transrectal ultrasound-guided prostate biopsy (TRUSPB) are increasing. The aim of this study was to evaluate the effectiveness of fosfomycin tromethamine (FMT) prophylaxis in preventing post-TRUSPB infectious complications. This nested case-control study included patients undergoing TRUSPB in a Canadian tertiary-care hospital who developed post-TRUSPB bacteraemia or urinary tract infection. Four prophylaxis periods were defined: (i) ciprofloxacin, low-resistance period (CIPRO-LOW), 2002-2009; (ii) ciprofloxacin, high-resistance period (CIPRO-HIGH), 2010-October 2013; (iii) oral FMT, one dose (FOSFO1), December 2013-September 2015; and (iv) oral FMT, two doses (FOSFO2), November 2015-June 2016. Incidence rates of the infection were calculated. TRUSPB (n=9391) resulted in 138 cases of urinary sepsis (58% with bacteraemia). The incidence rates were 1.8% (CIPRO-HIGH), 3.5% (FOSFO1; P=0.004 vs. CIPRO-HIGH) and 2.7% (FOSFO2; P=0.19 vs. CIPRO-HIGH). Although Escherichia coli remained the predominant pathogen with fosfomycin-based regimens, the proportion of infections caused by Klebsiella spp. was higher (20/66; 30.3%) than with ciprofloxacin-based regimens (2/77; 2.6%; P<0.0001). Independent risk factors for infection were the prophylactic regimen administered, presence of urological co-morbidities and diabetes. FMT was therefore not an effective alternative to ciprofloxacin for preventing post-TRUSPB urinary sepsis. These results highlight the need for novel antibacterial prophylaxis approaches.

Identifiants

pubmed: 30553114
pii: S2213-7165(18)30237-6
doi: 10.1016/j.jgar.2018.11.020
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Fosfomycin 2N81MY12TE

Types de publication

Evaluation Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

112-116

Informations de copyright

Copyright © 2018 International Society for Chemotherapy of Infection and Cancer. Published by Elsevier Ltd. All rights reserved.

Auteurs

Alex Carignan (A)

Department of Microbiology and Infectious Diseases, Université de Sherbrooke, 3001 12e Avenue Nord, Sherbrooke, QC, J1H5N4, Canada; Centre de Recherche du Centre Hospitalier Universitaire de Sherbrooke, 3001 12e Avenue Nord, Sherbrooke, QC, J1H5N4, Canada. Electronic address: Alex.Carignan@USherbrooke.ca.

Robert Sabbagh (R)

Centre de Recherche du Centre Hospitalier Universitaire de Sherbrooke, 3001 12e Avenue Nord, Sherbrooke, QC, J1H5N4, Canada; Division of Urology, Department of Surgery, Université de Sherbrooke, 3001 12e Avenue Nord, Sherbrooke, QC, J1H5N4, Canada.

Vincent Masse (V)

Department of Microbiology and Infectious Diseases, Université de Sherbrooke, 3001 12e Avenue Nord, Sherbrooke, QC, J1H5N4, Canada.

Nicolas Gagnon (N)

Department of Microbiology and Infectious Diseases, Université de Sherbrooke, 3001 12e Avenue Nord, Sherbrooke, QC, J1H5N4, Canada.

Louis-Philippe Montpetit (LP)

Department of Microbiology and Infectious Diseases, Université de Sherbrooke, 3001 12e Avenue Nord, Sherbrooke, QC, J1H5N4, Canada.

Marc-Andre Smith (MA)

Department of Microbiology and Infectious Diseases, Université de Sherbrooke, 3001 12e Avenue Nord, Sherbrooke, QC, J1H5N4, Canada.

Mathieu Raymond (M)

Department of Internal Medicine, Université de Sherbrooke, 3001 12e Avenue Nord, Sherbrooke, QC, J1H5N4, Canada.

Catherine Allard (C)

Department of Microbiology and Infectious Diseases, Université de Sherbrooke, 3001 12e Avenue Nord, Sherbrooke, QC, J1H5N4, Canada.

Cybèle Bergeron (C)

Department of Microbiology and Infectious Diseases, Université de Sherbrooke, 3001 12e Avenue Nord, Sherbrooke, QC, J1H5N4, Canada.

Jacques Pépin (J)

Department of Microbiology and Infectious Diseases, Université de Sherbrooke, 3001 12e Avenue Nord, Sherbrooke, QC, J1H5N4, Canada; Centre de Recherche du Centre Hospitalier Universitaire de Sherbrooke, 3001 12e Avenue Nord, Sherbrooke, QC, J1H5N4, Canada.

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